Medline recalls hernia repair tote kits with Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use, making the product unusable for application.
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Medline is recalling hernia repair tote kits that contain a specific adhesive which can crack during use, rendering the product unusable. This affects kits with the model DYNJ90833: HERNIA REPAIR TOTE.
The adhesive in the kits may crack during use, which can make the product unusable for applying the hernia repair material. This could lead to the need for rework or additional procedures.
Hernia repair patients using the recalled Medline convenience kits with model DYNJ908337D are affected. Patients using the kits for surgical procedures are at higher risk.
Check for the model number DYNJ908337D on the Medline hernia repair tote kit. The kit was sold with UDI-DI 10198459409431 and lot number 25KBB755.
Look for the model number DYNJ908337D on the Medline hernia repair tote kit.
The kits contain a specific adhesive that may crack during use, rendering the product unusable for application.
Check for the model number DYNJ908337D on the Medline hernia repair tote kit. The kit was sold with UDI-DI 10198459409431 and lot number 25KBB755.
The official recall notice does not specify a remedy or action steps for the recalled kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2427-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2427-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
+ 1 more story
